Clinical Trial Scientist
Clinical Trial Scientist
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Job Description
Job Title: Clinical Trial Scientist
Job Location: Basildon UK
Job Location Type: Hybrid
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
Clinical Trial Scientist
Based in Basildon (hybrid role: 3 days office 2 days home per week)
Salary: Competitive Benefits Bonus
Permanent or FTC role
If you are an exceptional clinical trials professional looking for a new and varied role with a fastgrowing international business then we want to hear from you.
Join us to help improve peoples' lives and make healthcare better for everyone!
Why Pharmanovia
Pharmanovia is a dynamic fastgrowing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche triedandtrusted medicines.
Our core behaviours are:
- We act decisively but we never compromise on quality.
- We keep our promises and do as we say.
- We value our heritage and foster an entrepreneurial spirit.
- We reinvest in our future in our products our brands and our people.
- We give back to our communities.
Since its inception in 2013 Pharmanovia has grown consistently year on year focusing on delivering highquality branded prescription medicines to patients prescribers and healthcare providers across the world. Our growth has enabled the company to reinvest in its products brands people and to give back to its communities. A people business with a strong supportive culture that encourages innovation and entrepreneurial spirit our team comprises over 300 employees and 29 nationalities operating from offices in the UK Denmark Netherlands Switzerland U.A.E. India Singapore Italy Spain and South Korea.
We are an agile committed and innovative global specialty pharma business and a preferred partner for innovator pharma companies instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental social and governance considerations across the business and workforce.
Pharmanovia's therapeutic areas include Cardiovascular Oncology Endocrinology and Neurology.
About the role
Reporting to Head of Clinical Development you will play a key role in the design execution and oversight of clinical trials across various phases (IIV). This position collaborates with crossfunctional teams including Regulatory Affairs Market Access Strategic Marketing Legal and Medical Affairs to ensure scientific integrity and operational excellence in clinical trial planning and execution.
You will contribute to protocol development data analysis and scientific communication to drive clinical development strategies and achieve highquality outcomes that meet regulatory and corporate standards. You will also act as the main point of interaction with external CROs help in identifying best partners to appoint for trial execution and support as well as ensuring each clinical study protocol is designed with scientific integrity with the endpoints clearly addressing the study objectives in line with the CDP and business needs and other regulatory standards of all trials including IITs.
The department has an ethos of continuous improvement refining systems and creating efficiencies. This along with the rapid growth of the business leads to a varied and dynamic working environment.
Main responsibilities and duties
Clinical Trial Design:
- Develop and contribute to the design and writing of clinical trial protocols investigator brochures and related study documents.
- Collaborate with the clinical development team to establish study objectives endpoints and inclusion/exclusion criteria.
- Provide scientific input into trial design statistical analysis and risk management strategies.
Study Execution and Oversight:
- Ensure trials are conducted in compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Oversee data collection quality control and data integrity throughout the trial lifecycle.
- Serve as a point of contact for clinical trial sites supporting trialrelated activities troubleshooting and monitoring patient safety.
Data Analysis and Reporting:
- Analyse and interpret clinical data working closely with biostatistics and data management teams to ensure data accuracy.
- Contribute to the preparation of clinical study reports (CSRs) abstracts posters and manuscripts for internal and external presentations.
- Review study results for accuracy and consistency identifying key findings relevant to product development.
CrossFunctional Collaboration:
- Partner with Medical Affairs Regulatory Affairs Market Access and Pharmacovigilance to ensure alignment on study objectives and milestones.
- Provide scientific expertise in meetings with key stakeholders including regulatory bodies investigators and partners.
- Contribute to project timelines budget adherence and risk management.
Regulatory Support:
- Assist in the preparation of regulatory submissions including PIP and MAAs by providing scientific insights and data.
- Stay current with regulatory guidelines therapeutic area trends and competitive landscape to inform clinical development strategies.
About you what you will need to have
- Advanced degree (Ph.D. or equivalent) in life sciences clinical research or related field.
- Minimum 5 years of experience in clinical trial management.
- High level of scientific and analytical ability to design and interpret complex clinical studies.
- Ability to work crossfunctionally and foster strong partnerships within and outside the organization.
- Strong attention to protocol adherence data accuracy and scientific integrity.
- Effective problemsolving skills with a proactive approach to identifying and addressing trial challenges.
- Strong knowledge of GCP ICH guidelines and relevant regulatory requirements.
- Excellent communication and presentation skills with an ability to translate complex scientific information for diverse audiences.
- Determined driven to achieve results and business minded.
- Proven track record of working and leading a crossfunctional team in a matrix environment.
- The ability to review both data and procedures in detail and the ability to see the greater overall picture.
What we offer
We offer a competitive salary plus bonus and rewards package including holiday health & wellbeing program employee recognition awards social events pension scheme and hybrid working.
By applying for this role your details will be sent to Ortolan People who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants this may not be possible.
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Employment Type
Full Time
